FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

SUNRISE CURING LAMP

K Number: K962192 · Decision Sep 3, 1996
Classifications
1
FEI Numbers
204
Registration Numbers
204
Same Product Code
931
Applicant Total
18
Review Days
88

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Basic Information

Device Name
SUNRISE CURING LAMP
K Number
K962192
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3690
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Sunrise Technologies, Inc.
Date Received
June 7, 1996
Decision Date
September 3, 1996
Product Code
EBF
Advisory Committee
Dental
Review Advisory Committee
DE
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
EBF Material, Tooth Shade, Resin

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Other Clearances by Sunrise Technologies, Inc.

K Number Device Name
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K933017 MODEL 5030 SUCTION HANDPIECE SYSTEM
K931774 UPGRADED PACKAGE FOR DLASE 300 PULSED DENTAL LASER
K930789 8-WATT PULSED DENTAL LASER SYSTEM
K930879 2.5 WATT PULSED DENTAL LASER SYSTEM
K925549 SLASE 210 PLUS HOLMIUM LASER SYSTEM
K920248 MODEL SLASE 210 HOLMIUM LASER SYSTEM
K920107 ADL 800 ND:YAG LASER SYSTEM FOR INTRAORAL TIS. SUR
Search all 18 clearances from Sunrise Technologies, Inc. →